Shiraishi Kazushige, Shichino Shigeyuki, Ueha Satoshi, Nakajima Takuya, Hashimoto Shinichi, Yamazaki Satoshi, Matsushima Kouji
Department of Molecular Preventive Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan; Division of Molecular Regulation of Inflammatory and Immune Diseases, Research Institute of Biomedical Sciences, Tokyo University of Science, Noda 278-0022, Japan.
Department of Molecular Preventive Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan; Division of Molecular Regulation of Inflammatory and Immune Diseases, Research Institute of Biomedical Sciences, Tokyo University of Science, Noda 278-0022, Japan; Department of Integrative Medicine for Longevity, Graduate School of Medical Sciences, Kanazawa University, Kanazawa 920-8641, Japan.
iScience. 2019 Jan 25;11:318-333. doi: 10.1016/j.isci.2018.12.022. Epub 2018 Dec 26.
Lung epithelial cells and fibroblasts are key cell populations in lung development. Fibroblasts support type 2 alveolar epithelial cells (AEC2) in the developing and mature lung. However, fibroblast-AEC2 interactions have not been clearly described. We addressed this in the present study by time course serial analysis of gene expression sequencing (SAGE-seq) of epithelial cells and fibroblasts of developing and mature murine lungs. We identified lung fibroblast-epithelial interactions that potentially regulate alveologenesis and are mediated by fibroblast-expressed ligands and epithelial cell surface receptors. In the epithelial-fibroblast co-culture alveolosphere formation assay, single intervention against fibroblast-expressed ligand or associated signaling cascades promoted or inhibited alveolosphere growth. Adding the ligand-associated molecules fibroblast growth factor 7 and Notch ligand and inhibitors of bone morphogenetic protein 4, transforming growth factor β, and glycogen synthase kinase-3β to the culture medium enabled fibroblast-free alveolosphere formation. The results revealed the essential factors regulating fibroblast-AEC2 interactions.
肺上皮细胞和成纤维细胞是肺发育中的关键细胞群体。在发育中的和成熟的肺中,成纤维细胞支持2型肺泡上皮细胞(AEC2)。然而,成纤维细胞与AEC2之间的相互作用尚未得到明确描述。在本研究中,我们通过对发育中和成熟的小鼠肺上皮细胞和成纤维细胞进行基因表达测序(SAGE-seq)的时间进程序列分析来解决这一问题。我们确定了肺成纤维细胞与上皮细胞之间的相互作用,这些相互作用可能调节肺泡形成,并由成纤维细胞表达的配体和上皮细胞表面受体介导。在上皮-成纤维细胞共培养肺泡球形成试验中,单独针对成纤维细胞表达的配体或相关信号级联进行干预可促进或抑制肺泡球生长。向培养基中添加配体相关分子成纤维细胞生长因子7和Notch配体以及骨形态发生蛋白4、转化生长因子β和糖原合酶激酶-3β的抑制剂可实现无成纤维细胞的肺泡球形成。结果揭示了调节成纤维细胞与AEC2相互作用的关键因素。